Why the study?
Do nanoparticle-based imaging agents improve the early diagnosis of endothelial dysfunction in atherosclerosis and cancer?
Do nanoparticle-based imaging agents improve the early diagnosis of endothelial dysfunction in atherosclerosis and cancer?
Nanoparticle-based multimodal imaging agents hold significant potential for the early molecular-level detection and diagnosis of endothelial dysfunction in atherosclerosis and cancer.
Supports hypothesis generation for multimodal nanoparticle imaging; leaves open clinical translation for early atherosclerosis and cancer diagnosis.
Endothelium plays a vital role in various vascular functions, and its dysfunction is a key underlying process closely related to diverse array of diseases such as atherosclerosis and tumor. Therefore, early detection of endothelial dysfunction at the functional or molecular level is of high importance for effective therapy. Recent advances in nanotechnology and our understanding in cellular and molecular biology have provided various biomedical imaging modalities and nanosized multimodal imaging agents. Multimodal nanoparticles that encompass the targeting ligands and magnetic/optical imaging labels enable us to visualize the pathophysiological process of various diseases using multiple imaging techniques. To visualize the specific pathogenic process at the molecular level, the imaging probe needs to be surface-functionalized with specific affinity ligands such as monoclonal antibodies (mAb). Combining the functional imaging agents along with therapeutic drugs has great potential for effective early detection, accurate diagnosis, and treatment of disease. The current review will highlight the application of various nanoparticle-based imaging agents and their recent developments in diagnosing endothelium dysfunction with a special emphasis on atherosclerosis and cancer.
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Saravanakumar et al. (2009) studied this question.
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